Canonical Allele Identifier: CA2270161234

Gene: SCN4A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63942029G= , CM000679.2:g.63942029G=	GRCh38
NC_000017.10:g.62019389G= , CM000679.1:g.62019389G=	GRCh37
NC_000017.9:g.59373121G=	NCBI36
NG_011699.1:g.35890C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435607.3:c.4289-36C= MANE Select	ENSP00000396320.1:n.4289-36C=
ENST00000578147.5:c.4289-36C=	ENSP00000463963.1:n.4289-36C=
NM_000334.4:c.4289-36C= MANE Select	NP_000325.4:n.4289-36C=
XM_005257566.3:c.4289-36C=	XP_005257623.1:n.4289-36C=